rs121917867

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121917867(C;G)

Make rs121917867(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

56453703

Gene

MIP

is a	snp
is	mentioned by
dbSNP	rs121917867
dbSNP (classic)	rs121917867
ClinGen	rs121917867
ebi	rs121917867
HLI	rs121917867
Exac	rs121917867
Gnomad	rs121917867
Varsome	rs121917867
LitVar	rs121917867
Map	rs121917867
PheGenI	rs121917867
Biobank	rs121917867
1000 genomes	rs121917867
hgdp	rs121917867
ensembl	rs121917867
geneview	rs121917867
scholar	rs121917867
google	rs121917867
pharmgkb	rs121917867
gwascentral	rs121917867
openSNP	rs121917867
23andMe	rs121917867
SNPshot	rs121917867
SNPdbe	rs121917867
MSV3d	rs121917867
GWAS Ctlg	rs121917867

Max Magnitude

0

ClinVar
Risk	rs121917867(G;G) rs121917867(T;T)
Alt	rs121917867(G;G) rs121917867(T;T)
Reference	Rs121917867(C;C)
Significance	Pathogenic
Disease	Cataract 15
Variation	info
Gene	MIP
CLNDBN	Cataract 15, multiple types
Reversed	1
HGVS	NC_000012.11:g.56847487G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015428.26,